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首页> 外文期刊>Journal of nanoscience and nanotechnology >Construction of a novel peptide nucleic acid piezoelectric gene sensor microarray detection system
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Construction of a novel peptide nucleic acid piezoelectric gene sensor microarray detection system

机译:新型肽核酸压电基因传感器微阵列检测系统的构建

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A novel 2 x 5 clamped style piezoelectric gene sensor microarray has been successfully constructed. Every crystal unit of the fabricated gene sensor can oscillate independently without interfering with each other. The bis-peptide nucleic acid (bis-PNA) probe, which can combine with target DNA or RNA sequences more effectively and specifically than a DNA probe, was designed and immobilized on the surface of the gene sensor microarray to substitute the conventional DNA probe for direct detection of the hepatitis B virus (HBV) genomic DNA. Detection conditions were then explored and optimized. Results showed that PBS buffer of pH 6.8, an ion concentration of 20 mmol/liter, and a probe concentration of 1.5 mu mol/liter were optimal for the detection system. Under such optimized experimental conditions, the specificity of bis-PNA was proved much higher than that of DNA probe. The relationship between quantity of target and decrease of frequency showed a typical saturation curve when concentrations of target HBV DNA varied from 10 pg/liter to 100 mu g/liter, and 10 mu g/liter was the watershed, with a statistic linear regression equation of I gC = -2.7455 + 0.0691 Delta F and the correlating coefficient of 0.9923. Fortunately, this is exactly the most ordinary variant range of the HBV virus concentration in clinical hepatitis samples. So, a good technical platform is successfully constructed and it will be applied to detect HBV quantitatively in clinical samples.
机译:一种新型的2 x 5钳位型压电基因传感器微阵列已成功构建。所制造的基因传感器的每个晶体单元都可以独立振荡,而不会互相干扰。设计了双肽核酸(bis-PNA)探针,该探针可比DNA探针更有效地结合靶DNA或RNA序列,并将其固定在基因传感器微阵列的表面上,以取代传统的DNA探针。直接检测乙肝病毒(HBV)基因组DNA。然后探索和优化检测条件。结果表明,pH 6.8,离子浓度为20 mmol / L,探针浓度为1.5μmol/ L的PBS缓冲液最适合用于检测系统。在这种优化的实验条件下,证明了bis-PNA的特异性远高于DNA探针。当目标HBV DNA的浓度从10 pg / l变化到100μg/ l,以10μg/ l为分界时,目标数量与频率降低之间的关系显示出一条典型的饱和曲线,具有统计线性回归方程I gC的系数= -2.7455 + 0.0691 Delta F,相关系数为0.9923。幸运的是,这恰恰是临床肝炎样本中HBV病毒浓度最普通的变异范围。因此,成功构建了良好的技术平台,并将其用于定量检测临床样本中的HBV。

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